Scene: Figure 4
WU-Minn HCP Consortium Open Access Data Use Terms
1. I will not attempt to establish the identity of or attempt to contact any of the included human subjects.
2. I understand that under no circumstances will the code that would link these data to Protected Health Information be given to me, nor will any additional information about individual human subjects be released to me under these Open Access Data Use Terms.
3. I will comply with all relevant rules and regulations imposed by my institution. This may mean that I need my research to be approved or declared exempt by a committee that oversees research on human subjects, e.g. my IRB or Ethics Committee. The released HCP data are not considered de-identified, insofar as certain combinations of HCP Restricted Data (available through a separate process) might allow identification of individuals. Different committees operate under different national, state and local laws and may interpret regulations differently, so it is important to ask about this. If needed and upon request, the HCP will provide a certificate stating that you have accepted the HCP Open Access Data Use Terms.
4. I may redistribute original WU-Minn HCP Open Access data and any derived data as long as the data are redistributed under these same Data Use Terms.
5. I will acknowledge the use of WU-Minn HCP data and data derived from WU-Minn HCP data when publicly presenting any results or algorithms that benefitted from their use.
1. Papers, book chapters, books, posters, oral presentations, and all other printed and digital presentations of results derived from HCP data should contain the following wording in the acknowledgments section: "Data were provided [in part] by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University."
2. Authors of publications or presentations using WU-Minn HCP data should cite relevant publications describing the methods used by the HCP to acquire and process the data. The specific publications that are appropriate to cite in any given study will depend on what HCP data were used and for what purposes. An annotated and appropriately up-to-date list of publications that may warrant consideration is available at http://www.humanconnectome.org/about/acknowledgehcp.html
3. The WU-Minn HCP Consortium as a whole should not be included as an author of publications or presentations if this authorship would be based solely on the use of WU-Minn HCP data.
6. Failure to abide by these guidelines will result in termination of my privileges to access WU-Minn HCP data.
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HCP group average resting-state fMRI reproducibility. Here we show the reproducibility of Resting State Networks (RSNs, ICA d=137) and dense Functional Connectivity maps. The odd rows are the 210P dataset and the even rows are the 210V dataset. The RSNs were produced using ICA on the 210P dataset and then weighted regression of the group spatial maps onto the individual subject dense timeseries to produce individual subject spatial maps in all 449 subjects. The individual subject maps were then separately averaged across the 210P and 210V groups. The top two rows show the left lateralized language network and the next two rows show its right hemisphere homologue, both scaled between beta=+/-0.2. The next two rows show dense functional connectivity (FC) of the bilateral task negative (default mode) network seeded from a posterior inferior parietal grayordinate (green arrow, white sphere on left lateral surface), which has strong anti-correlation with the task positive network. The last two rows show the early visual network seeded from a grayordinate in the center of the calcarine sulcus (purple arrow, white sphere on left medial surface), which shows positive correlation with the entire brain. The dense FC maps are scaled from r=-0.8 to 0.8.
Surface Mesh:32k fs LR, Registration:MSMAll, Species:Human, Modality:Myelin Map, Modality:T1-weighted, Modality:T2-weighted